Canonical Allele Identifier: CA2684812660

Gene: FLNC

Linked Data

• gnomAD v4: 7-128841131-C-CTGA

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128841134_128841136dup , CM000669.2:g.128841134_128841136dup	GRCh38
NC_000007.13:g.128481188_128481190dup , CM000669.1:g.128481188_128481190dup	GRCh37
NC_000007.12:g.128268424_128268426dup	NCBI36
NG_011807.1:g.15706_15708dup , LRG_870:g.15706_15708dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.1814-36_1814-34dup MANE Select	ENSP00000327145.8:n.1814-36_1814-34dup
ENST00000325888.12:c.1814-36_1814-34dup	ENSP00000327145.8:n.1814-36_1814-34dup
ENST00000346177.6:c.1814-36_1814-34dup	ENSP00000344002.6:n.1814-36_1814-34dup
NM_001127487.1:c.1814-36_1814-34dup	NP_001120959.1:n.1814-36_1814-34dup
NM_001458.4:c.1814-36_1814-34dup , LRG_870t1:c.1814-36_1814-34dup	NP_001449.3:n.1814-36_1814-34dup
NM_001127487.2:c.1814-36_1814-34dup	NP_001120959.1:n.1814-36_1814-34dup
NM_001458.5:c.1814-36_1814-34dup MANE Select	NP_001449.3:n.1814-36_1814-34dup